Canonical Allele Identifier: CA399605374

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723621A>C (hg19) ; chr17:g.42571603A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571603A>C , CM000679.2:g.42571603A>C	GRCh38
NC_000017.10:g.40723621A>C , CM000679.1:g.40723621A>C	GRCh37
NC_000017.9:g.37977147A>C	NCBI36
NG_029442.1:g.9544A>C
NG_031960.1:g.11229T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.735A>C MANE Select	ENSP00000416627.1:p.Ter245Cys
ENST00000246912.8:c.897A>C	ENSP00000246912.3:p.Ter299Cys
ENST00000346833.8:c.645A>C	ENSP00000320913.3:p.Ter215Cys
ENST00000435881.6:c.735A>C	ENSP00000416627.1:p.Ter245Cys
ENST00000585403.5:n.942A>C
ENST00000588320.1:n.1211A>C
ENST00000590050.5:n.901A>C
NM_170607.2:c.897A>C	NP_733752.1:p.Ter299Cys
NM_198204.1:c.735A>C	NP_937847.1:p.Ter245Cys
NM_198205.1:c.645A>C	NP_937848.1:p.Ter215Cys
NM_198204.2:c.735A>C MANE Select	NP_937847.1:p.Ter245Cys
NM_170607.3:c.897A>C	NP_733752.1:p.Ter299Cys
NM_198205.2:c.645A>C	NP_937848.1:p.Ter215Cys